EP0555879A1 - Composition de revêtement et son procédé de préparation - Google Patents

Composition de revêtement et son procédé de préparation Download PDF

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Publication number
EP0555879A1
EP0555879A1 EP93102278A EP93102278A EP0555879A1 EP 0555879 A1 EP0555879 A1 EP 0555879A1 EP 93102278 A EP93102278 A EP 93102278A EP 93102278 A EP93102278 A EP 93102278A EP 0555879 A1 EP0555879 A1 EP 0555879A1
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group
component
weight
parts
carbon atoms
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EP93102278A
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German (de)
English (en)
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EP0555879B1 (fr
Inventor
Toshinori Sakagami
Koichi Nagano
Tomonobu Shimizu
Kinji Yamada
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JSR Corp
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Japan Synthetic Rubber Co Ltd
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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
    • C09D183/04—Polysiloxanes

Definitions

  • the present invention relates to a coating composition, and, in particular, to a coating composition with superior storage stability which is suitable for forming a coating film with superior performance on the surface of substrates made of stainless steel, aluminum, ceramics, cement, paper, glass, plastic, inorganic ceramic, and on cloth, or the like.
  • a coating composition as disclosed in Japanese Patent Laid-open (ko-kai) No. 135465/1985, comprising a dispersion of a partial condensate of an organosilane with a colloidal silica and a silicon-denatured acryl resin; a coating composition as disclosed in Japanese Patent Laid-open (ko-kai) No.1769/1989 comprising a composition formed from a condensation product of an organosilane with a chelated zirconium alkoxide compound and a vinyl resin containing a hydrolyzable silyl group; or a coating composition as disclosed in US Patent 4,904,721 comprising a composition formed from a condensate of organosilane, colloidal alumina and a vinyl resin containing hydrolyzable silyl group.
  • composition disclosed in Japanese Patent Laid-open (ko-kai) No. 1769/1989 exhibits inadequate stability in storage and, if its solid content is increased, tends to form a gel over in a short period of time.
  • an object of the present invention is to provide, with due consideration to the drawbacks of such conventional compositions, a coating composition with superior stability during storage, excellent transparency, and superb adhesion, and which can form a coating film with superior resistance to heat, moisture, sea water, organic chemicals, acids, alkalis, corrosion, abrasion, weathering, humidity, and the like, and which has a high degree of hardness and excellent adherence.
  • the component (a) is a hydrolyzate and/or a partial condensate obtained by hydrolyzing and condensing an organosilane (a') represented by formula R1Si(OR2)3 and is employed as a binder in the composition of the present invention.
  • component (a) is a partial condensate of organosilane (a') and has a weight average molecular weight, in terms of polystyrene, of 500 to 50,000.
  • R1 in the organosilane (a') is an organic group with 1 to 8 carbon atoms such as, for example, alkyl group such as methyl group, ethyl group, n-propyl group, i-propyl group, or can also be gamma -chloropropyl group, vinyl group, 3,3,3-trifluoropropyl group, gamma -glycidoxypropyl group, gamma -methacryloxypropyl group, gamma -mercaptopropyl group, phenyl group, 3,4-epoxycyclohexylethyl group, or the like.
  • alkyl group such as methyl group, ethyl group, n-propyl group, i-propyl group
  • R1 in the organosilane (a') is an organic group with 1 to 8 carbon atoms such as, for example, alkyl group such as methyl group, ethyl group,
  • R2 in the organosilane (a') is an alkyl group with 1 to 5 carbon atoms or an acyl group with 1 to 4 carbon atoms such as, for example, methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group, sec-butyl group, tert-butyl group, acetyl group, or the like.
  • organosilane (a') examples include methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, n-propyltrimethoxysilane, n-propyltriethoxysilane, i-propyltrimethoxysilane, i-propyltriethoxysilane, gamma -chloropropyltrimethoxysilane, gamma -chloropropyltriethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, 3,3,-triphloropropyltrimethoxysilane, 3,3,3-trifluoropropyltriethoxysilane, gamma -glycidoxypropyltrimethoxysilane, gamma -glycidoxypropyltriethoxysilane, gamma
  • the preferable organosilanes (a') are methyltrimethoxysilane and methyltriethoxysilane.
  • Either one type of the organosilane (a') can be used independently or two or more types may be used in combination. It is preferable that 80 mol% or more of the organosilane (a') be CH3Si(OR2)3.
  • the component (b) is a hydrolyzate and/or a partial condensate obtained by hydrolyzing and condensing diorganosilane (b') represented by formula R12Si(OR2)2, wherein R1 and R2 are the same as for component (a) above, and is employed as a binder and also to make the coating film flexible and to improve the resistance to alkalis of the composition obtained in the present invention.
  • R1 and R2 in the organosilane (a') apply to R1 and R2 in the diorganosilane (b').
  • diorganosilane (b') include dimethyldimethoxysilane, dimethyldiethoxysilane, diethyldimethoxysilane, diethyldiethoxysilane, di-n-propyldimethoxysilane, di-n-propyldiethoxysilane, di-i-propyldimethoxysilane, di-i-propyldiethoxysilane, diphenyldimethoxysilane, diphenyldiethoxysilane, and the like.
  • the preferable diorganosilanes (b') are dimethyldimethoxysilane and dimethyldiethoxysilane. Either one type of diorganosilane (b') can be used independently or two or more types can be used together.
  • the component (b) is used in the composition of the present invention in the amount of 0 to 150 parts by weight, preferably 5 to 100 parts by weight, and most preferably 10 to 60 parts by weight, to 100 parts by weight of component (a'). If the amount exceeds 150 parts by weight, the adhesion and the curing characteristics of the resulting coating film are reduced.
  • the component (c), which is a vinyl resin containing a silyl group, is formed from a vinyl polymer as a main chain, and contains at least one, and preferably two or more, silyl group containing a silicon atom linked to a hydrolyzable group and/or a hydroxyl group at the end or in a side chain in one polymer molecule.
  • silyl groups are shown by formula: wherein X is a hydrolyzable group, such as halogen atom, alkoxy group, acyloxy group, aminoxy group, phenoxy group, thioalkoxy group, or amino group, or a hydroxyl group; R6 is a hydrogen atom, an alkyl group with 1 to 10 carbon atoms or an aralkyl group with 1 to 10 carbon atoms; and n is an integer from 1 to 3.
  • X is a hydrolyzable group, such as halogen atom, alkoxy group, acyloxy group, aminoxy group, phenoxy group, thioalkoxy group, or amino group, or a hydroxyl group
  • R6 is a hydrogen atom, an alkyl group with 1 to 10 carbon atoms or an aralkyl group with 1 to 10 carbon atoms
  • n is an integer from 1 to 3.
  • This component may be prepared, for example, by (i) reacting a hydrosilane compound and a vinyl resin which has a carbon-carbon double bond, or by (ii) polymerizing a silane compound represented by formula: wherein X, R6, and n are the same as above; and R7 is an organic group with a polymerizable double bond, with a vinyl compound.
  • hydrosilane compounds used in the above-mentioned manufacturing method (i) include hydrosilanes such as methyldichlorosilane, trichlorosilane, phenyldichlorosilane, and the like; alkoxysilanes such as methyldiethoxysilane, methyldimethoxysilane, phenyldimethoxysilane, trimethoxysilane, triethoxysilane, and the like; acyloxysilanes such as methyldiacetoxysilane, phenyldiacetoxysilane, triacetoxysilane, and the like; and aminosilanes such as methyldiaminoxysilane, triaminoxysilane, dimethylaminoxysilane, triaminosilane, and the like.
  • hydrosilanes such as methyldichlorosilane, trichlorosilane, phenyldichlorosilane,
  • vinyl resins containing a hydroxyl group there are no particular restrictions as to the vinyl resin used in the above-mentioned manufacturing method (i) with the exception of vinyl resins containing a hydroxyl group.
  • Preferred vinyl resins are copolymers of vinyl compounds, for example, (meth)acrylates such as methyl(meth)acrylate, ethyl(meth)acrylate, butyl(meth)acrylate, 2-ethylhexyl(meth)acrylate, cyclohexyl(meth)acrylate, and the like; carboxylic acids such as (meth)acrylic acid, itaconic acid, fumaric acid, and the like; acid anhydrides such as maleic anhydride, and the like; epoxy compounds such as glycidyl(meth)acrylate; amino compounds such as diethylaminoethyl(meth)acrylate, aminoethyl vinyl ether, and the like; amide compounds such as (meth)acrylamide, itac
  • vinyl compounds containing a hydroxyl group such as 2-hydroxyethyl(meth)acrylate, 2-hydroxypropyl-(meth)acrylate, 2-hydroxyvinyl ether, N-methylolacrylamide, and the like can also be used.
  • R8 is a hydrogen atom or a methyl group
  • R9 is an alkyl group with 1 to 6 carbon atoms such as methyl group, ethy
  • the number average molecular weight of the vinyl resin containing a silyl group (c), in terms of polystyrene, is in the range of 2,000 to 100,000, and preferably 4,000 to 50,000.
  • the vinyl resin containing a silyl group (c) is used in the composition of the present invention in the amount of 2 to 300 parts by weight, preferably 5 to 200 parts by weight, and most preferably 10 to 100 parts by weight, to 100 parts by weight of the organosilane (a') which is the raw material for component (a). If the amount is less than 2 parts by weight, the alkali resistance of the resulting coating film is reduced; if greater than 300 parts by weight, the weather resistance is poor.
  • Metal chelate compound (d) of the present invention is at least one metal chelate compound selected from a group of compounds represented by formulas Zr(OR3) p (R4COCHCOR5) 4-p , Ti(OR3) q (R4COCHCOR5) 4-q , and Al(OR3) r (R4COCHCOR5) 3-r .
  • This component is considered to promote the condensation reaction among the above-mentioned components (a) and (b) and the vinyl resin containing a silyl group (c), so that components (a) and (b) form a copolymer with component (c).
  • R3 and R4 are the same or different alkyl groups with 1 to 6 carbon atoms. Specific examples include ethyl group, n-propyl group, i-propyl group, n-butyl group, sec-butyl group, t-butyl group, n-pentyl group, phenyl group, and the like.
  • R5 is an alkyl group with 1 to 6 carbon atoms or an alkoxy group with 1 to 16 carbon atoms, such as, for example, methoxy group, ethoxy group, n-propoxy group, i-propoxy group, n-butoxy group, sec-butoxy group, t-butoxy group, lauryl group, stearyl group, and the like.
  • p and q are integers from 0 to 3; and r is an integer from 0 to 2.
  • the metal chelate compound (d) include zirconium chelate compounds such as tri-n-butoxyethylacetoacetate zirconium, di-n-butoxy ⁇ bis(ethylacetoacetate) zirconium, n-butoxytris(ethylacetoacetate) zirconium, tetrakis(n-propylacetoacetate) zirconium, tetrakis(acetylacetoacetate) zirconium, tetrakis(ethylacetoacetate) zirconium, and the like; titanium chelate compounds such as diisopropoxy ⁇ bis(ethylacetoacetate) titanium, diisopropoxy ⁇ bis(acetylacetonate) titanium, and the like; and aluminum chelate compounds such as diisopropoxyethylacetoacetate aluminum, diisopropoxyacetylacetonate aluminum, isopropoxy ⁇ bis(ethylacetoacetate) aluminum, isopropoxy ⁇ bis(e
  • tri-n-butoxyethylacetoacetate zirconium, diisopropoxy ⁇ bis(acetylacetonate) titanium, diisopropoxyethylacetoacetate aluminum, and tris(ethylacetoacetate) aluminum are preferable.
  • One type of the above metal chelate compounds (d) can be used independently or two or more types can be used in combination.
  • partially hydrolyzed compounds of these metal chelate compounds can also be used as component (d).
  • the metal chelate compound (d) is used in the composition of the present invention in the amount of 0.01 to 50 parts by weight, preferably 0.1 to 50 parts by weight, and most preferably 0.5 to 10 parts by weight, to 100 parts by weight of organosilane (a') which is the raw material for component (a). If the amount is less than 0.01 parts by weight, the formation of a copolymer of components (a) and (b) with component (c) is inadequate and the weather resistance of the coating film is impaired; if greater than 50 parts by weight, the storage stability of the composition deteriorates and undesirable cracks may be produced in the resulting coating film.
  • Organic solvent (e) of the present invention is mainly used to homogeneously blend components (a) to (d), and to adjust the solid portion of the composition so that various coating methods can be applicable to the composition. At the same time, it improves the dispersion stability and the storage stability of the composition.
  • organic solvent used as component (e) there are no particular restrictions as to the organic solvent used as component (e), so long as it can homogeneously mix components (a) to (d).
  • Suitable solvents are, for example, alcohols, aromatic hydrocarbons, ethers, ketones, esters, and the like.
  • alcohols used as the solvent include monohydric and dihydric alcohols. Of the monohydric alcohols, saturated aliphatic alcohols with 1 to 8 carbon atoms are preferable. Specific examples of these alcohols include methanol, ethanol, n-propyl alcohol, i-propyl alcohol, n-butyl alcohol, sec-butyl alcohol, tert-butyl alcohol, ethylene glycol, diethylene glycol, triethylene glycol, ethylene glycol monobutyl ether, acetic acid ethylene glycol monoethyl ether, and the like.
  • aromatic hydrocarbons used as the solvent include benzene, toluene, xylene, and the like.
  • ethers include tetrahydrofuran, dioxane, and the like.
  • ketones include acetone, methyl ethyl ketone, methyl isobutyl ketone, diisobutyl ketone, and the like.
  • esters include ethyl acetate, propyl acetate, butyl acetate, propylene carbonate, and the like.
  • One type of organic solvent (e) can be used independently or two or more types can be used together.
  • organic solvent (e) used in the composition There are no particular restrictions as to the amount of organic solvent (e) used in the composition. Usually, an amount is determined so as to adjust the concentration of the total solid portion depending on the application to which the composition is directed.
  • Component (f) is a type of ⁇ -diketone and/or ⁇ -ketoester represented by formula R4COCH2COR5 and is used as an agent for improving the stability of the composition of the present invention.
  • component (f) is presumed to coordinate with the metal atoms in the metal chelate compounds (d) (zirconium, titanium and/or aluminum compounds) present in the composition, which mainly comprises the above-mentioned (a) to (e) components, and to act so as to suppress the action of the metal chelate compounds for promoting the condensation reaction of the components (a) and (b) with the component (c), thus improving the storage stability of the resulting composition.
  • R4 and R5 in component (f) are the same as R4 and R5 in metal chelate compound (d).
  • ⁇ -diketone and/or ⁇ -ketoester (f) include acetylacetone, methyl acetoacetate, ethyl acetoacetate, n-propyl acetoacetate, i-propyl acetoacetate, n-butyl acetoacetate, sec-butyl acetoacetate, t-butyl acetoacetate, 2,4-hexanedione, 2,4-heptanedione, 3,5-heptanedione, 2,4-octanedione, 2,4-nonanedione, 5-methylhexanedione, and the like.
  • ⁇ -diketone and/or ⁇ -ketoester (f) can be used independently or two or more types can be used together.
  • This type of ⁇ -diketone and/or ⁇ -ketoester (f) is used in an amount of two or more mols, and preferably 3 to 20 mols, for one mol of metal chelate compound (d). If less than two mols, the storage stability of the resulting composition may be poor.
  • Components (a) to (f) are the main components of the composition of the present invention.
  • a composition comprising components (a) to (e) [composition (I)] is first produced, and to this composition (I) a required amount of component (f) is added to obtain the composition of the present invention.
  • water (g) is added for the hydrolysis and condensation of organosilane (a'), which is a component forming component (a), and/or diorganosilane (b'), which a component forming component (b).
  • the amount of water (g) used is normally 1.2 to 3.0 mols, and preferably 1.3 to 2.0 mols, for one mol of organosilane (a'), and normally 0.8 to 2.0 mols, and preferably about 0.9 to 1.5 mols, for one mol of diorganosilane (b').
  • the total solid concentration of the composition of the present invention comprising components (a) to (f) is preferably 50% by weight or less and can be suitably adjusted depending on the intended use of the composition.
  • the total solid concentration is normally 5 to 30% by weight.
  • the total solid concentration is normally 20 to 50% by weight, and preferably 25 to 40% by weight. If greater than 50% by weight, the storage stability of the composition is undesirably worsened.
  • a colloidal silica can be added to the composition of this invention to improve the hardness of the coating film.
  • types of colloidal silica which can be used for this purpose include an aqueous dispersion of colloidal silica, colloidal silica dispersed in an organic solvent such as methanol, isopropyl alcohol, or the like.
  • composition of the present invention it is also possible to add and disperse filler (h) in the composition of the present invention to provide highly specialized characteristics in the resulting coating film; e.g., coloration of the coating film, formation of a thick film, prevention of UV ray transmission to the undercoat, provision of anticorrosion properties, heat resistance, and the like.
  • filler (h) examples include water-insoluble pigments such as organic pigments, inorganic pigments, and the like; and other than pigments, metals and alloys; oxides, hydroxides, carbides, nitrides, sulfides, and the like of the metals and alloys, all in the shape of particles, fibers, or scales.
  • filler (h) in the shape of particles, fibers, or scales include iron, copper, aluminum, nickel, silver, zinc, ferrite, carbon black, stainless steel, silicon dioxide, titanium oxide, aluminum oxide, chromium oxide, manganese oxide, iron oxide, zircon, cobalt oxide, synthetic mullite, aluminum hydroxide, iron hydroxide, silicon carbide, silicon nitride, boron nitride, clay, kieselguhr, lime, gypsum, talc, barium carbonate, calcium carbonate, magnesium carbonate, barium sulfide, bentonite, mica, zinc green, chrome green, cobalt green, viridian, Guignet's green, cobalt-chrome green, Scheele green, green mud, manganese green, pigment green, ultramarine, Prussian blue, pigment blue, mountain blue, cobalt blue, cerulean blue, copper borate, molybdenum blue, copper sulfates,cobalt violet, mars
  • the average particle diameter or average length of filler (h) is normally 50 to 50,000 nm, and preferably 100 to 5,000 nm.
  • Filler (h) is used in the composition of the present invention in the amount of about 10 to 300 parts by weight to 100 parts by weight of the total solid portion of components (a) to (f).
  • a curing promoter may also be used according to the curing conditions to provide faster curing of the composition of the present invention.
  • the use of a curing agent is particularly effective when the composition is cured at a comparatively low temperature.
  • Examples of such a curing promoter include alkali metal salts of naphthenic acid, octylic acid, nitrous acid, sulfurous acid, aluminic acid, or the like; alkali compounds such as sodium hydroxide, potassium hydroxide, and the like; acidic compounds such as alkyl titanic acid, phosphoric acid, p-toluenesulfonic acid, phthalic acid, and the like; amine compounds such as ethylenediamine, hexanediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, piperidine, piperazine, m-phenylenediamine, ethanolamine, triethylamine, denatured amines used as an epoxy resin curing agent, gamma -aminopropyltriethoxysilane, gamma -(2-aminoethyl)aminopropyltrimethoxysilane, gamma -(2-amin
  • the curing promoter is normally used in the composition of the present invention in the amount of 0.1 to 15 parts by weight, and preferably 0.5 to 10 parts by weight, for 100 parts by weight of the solid portion of the composition of the present invention.
  • organic solvents other than the organic solvent (e) can be incorporated in the composition of the present invention.
  • Such organic solvents may be any solvents which do not induce precipitation when components (a) to (d) are mixed together, and include aliphatic hydrocarbons, aromatic hydrocarbons, halogenated hydrocarbons, ketones, esters, ethers, ketone ethers, ketone esters, ester ethers, and the like, as used in normal paints and coating agents.
  • Specific examples are benzene, toluene, xylene, methyl acetate, ethyl acetate, propyl acetate, butyl acetate, isoamyl acetate, and the like.
  • These organic solvents are normally used in an amount of about 100 parts by weight or less to 100 parts by weight of the composition of the present invention.
  • composition (I) containing components (a) to (e) is first prepared, and then component (f) is added to composition (I).
  • component (f) is added to composition (I).
  • the following methods (1) to (3) are examples of such methods which can preferable be employed.
  • a coating film can be formed by applying the composition of the present invention in a first application of a thickness of about 1 to 40 ⁇ m, followed by two or three additional applications of a thickness of about 2 to 80 ⁇ m, to the surface of the object substrate by brushing, spraying, or dipping, then drying at room temperature or heating for about 10 to 60 minutes at a temperature of about 30° to 200°C.
  • the substrate on which the composition is coated can be, for example, stainless steel, aluminum, ceramic, cement, paper, glass, plastic, inorganic ceramic substrates, cloth, and the like.
  • composition of the present invention When coating the composition of the present invention, it is possible to provide a primer of conventionally known acrylic resin, epoxy resin, urethane resin, polyester resin, or the like on the above substrate in advance in order to provide the substrate with better adhesion or smoothness, to give ornamental designs on the surface, or to offset the texture of porous materials.
  • the average molecular weight in terms of polystyrene was measured by gel permeation chromatography (GPC) under the following conditions.
  • the test material was prepared by dissolving one gram of organopolysiloxane in 100 cc of tetrahydrofuran solvent.
  • the storage stability was visually judged from the presence or absence of gel formation when the sample was stored in a tightly sealed polyethylene bottle without the addition of a curing promoter.
  • the viscosity of material in which no gelling occurred was measured in a BM model viscosimeter (manufactured by Tokyo Keiki Co., Ltd.). A material exhibiting a viscosity change of 20% or less was deemed to be unchanged.
  • the adhesion was measured by subjecting the sample three times to a cross-cut adhesion test in accordance with JIS K5400 followed by a tape peeling test. The average was taken as the adhesion of the test sample.
  • Hardness was based on pencil hardness in accordance with JIS K5400.
  • Resistance to alkali (1) was measured by adding one cc of ]-40% aqueous solutions of sodium hydroxide dropwise onto the coating film, allowing it to stand for 6 hours in a lidded laboratory dish, washing with water, then observing the condition of the coating film. The maximum concentration of an aqueous solution of sodium hydroxide which caused no abnormalities to the film was thus determined.
  • Resistance to alkali (2) was measured by immersing a substrate coated with the composition in a saturated aqueous solution of calcium hydroxide for 60 days, then observing the condition of the coating film.
  • Resistance to weathering was measured by conducting a 3,000 hour irradiation test in a weather meter in accordance with JIS K5400, then observing the condition of the coating film.
  • Resistance to organic chemicals was measured by adding 2 cc of isopropyl alcohol dropwise onto the coating film, wiping with a cloth after 5 minutes, then observing the condition of the coating film.
  • Resistance to humidity was measured by continuous storage for 1,000 hours at a temperature of 50°C under 95% relative humidity, then removing the sample and observing the condition of the coating film.
  • Resistance to hot water was measured by immersing the an inorganic substrate onto which the composition was coated in hot water at 60°C for 14 days, then observing the condition of the coating film.
  • Recovery from staining was measured by coating a paste made from a 1:2 mixture of carbon black and kerosene onto the coating film, holding it at room temperature for 24 hours, washing with water using a sponge, then observing the condition of recovery from staining of the coating film.
  • a sample with no staining was indicated by AAA, with slight staining by BBB, and with severe staining by CCC.
  • methyltrimethoxysilane (a') 100 parts of methyltrimethoxysilane (a'), 30 parts of dimethyldimethoxysilane (b'), 25 parts of ion exchanged water, and 0.01 part of a 0.1 N aqueous solution of hydrochloric acid were added to a reaction vessel equipped with a condenser and a stirrer, and blended. The mixture was heated with stirring to 60°C and reacted at this temperature for 3 hours to obtain a solution of organopolysiloxane (ii) with a solid concentration of 44%.
  • the number average molecular weight was determined to be 1,500.
  • compositions B to O given in Table 1 were also obtained.
  • Composition O was obtained by adding the components (a') to (f) simultaneously.
  • compositions A to L The storage stability of these compositions A to L, and the evaluation results for a test leaf obtained by coating the composition onto an alkali-defatted aluminum plate (JIS H4000, A1050P) to a dried thickness of 20 ⁇ m, then heating for 10 minutes at 150°C, are given in Table 1.
  • compositions A to M were added to compositions A to M in the quantities shown in Table 2, and the mixtures were kneaded using a sand mill to obtain compositions (a) to (k).
  • Coatings formed by blending compositions (a) to (k) with 2% dibutyltindilaurate as a curing agent were applied to substrates formed by coating Mighty Eposealer (an epoxy resin sealer manufactured by Dai Nippon Toryo Co., Ltd.) onto a slate plate (JIS A5043F) to give a dried weight of 50 gm/m2.
  • the coating composition of the present invention exhibits highly superior storage stability, is transparent, and has superior characteristics with respect resistance to heat, moisture, sea water, organic chemicals, acids, alkalis, corrosion, abrasion, weathering, humidity, and the like. It exhibits excellent adhesion and can form a coating film which has a high degree of hardness.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
EP93102278A 1992-02-13 1993-02-12 Composition de revêtement et son procédé de préparation Expired - Lifetime EP0555879B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP5882492 1992-02-13
JP58824/92 1992-02-13

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EP0555879A1 true EP0555879A1 (fr) 1993-08-18
EP0555879B1 EP0555879B1 (fr) 1997-05-07

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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0656409A3 (fr) * 1993-11-30 1996-04-17 Shinetsu Chemical Co Compositions de revêtement.
EP0722993A1 (fr) * 1993-08-06 1996-07-24 Dai Nippon Toryo Co., Ltd. Procédé de revêtement d'une tÔle d'acier
EP0824127A3 (fr) * 1996-08-14 1998-05-27 Japan Synthetic Rubber Co., Ltd. Composition sous forme de dispersion aqueuse
EP0844283A1 (fr) * 1996-11-20 1998-05-27 Japan Synthetic Rubber Co., Ltd. Compositions de résine durcissable et produits réticulés
US6100332A (en) * 1998-01-20 2000-08-08 Shin-Etsu Chemical Co., Ltd. Coating composition for electrifying members and electrophotographic carrier
EP1054047A3 (fr) * 1999-05-21 2001-10-10 JSR Corporation Composition de revêtement et films et verre revêtus par cette composition
EP1162247A3 (fr) * 2000-06-08 2002-04-17 Shin-Etsu Chemical Co., Ltd. Composition de revêtement, méthode pour revêtement et article revêtu
EP0921561A3 (fr) * 1997-12-02 2004-11-24 JSR Corporation Composition de revêtement pour la fabrication des couches
WO2007137971A2 (fr) 2006-05-26 2007-12-06 Cht R. Beitlich Gmbh Concentrés diluables dans l'eau pour l'application de revêtements sur différents substrats
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EP0824127A3 (fr) * 1996-08-14 1998-05-27 Japan Synthetic Rubber Co., Ltd. Composition sous forme de dispersion aqueuse
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KR100563507B1 (ko) * 1996-08-14 2007-01-31 제이에스알 가부시끼가이샤 수성분산체
US6313233B1 (en) 1996-11-20 2001-11-06 Japan Synthetic Rubber Co., Ltd. Curable resin composition cured products
EP0844283A1 (fr) * 1996-11-20 1998-05-27 Japan Synthetic Rubber Co., Ltd. Compositions de résine durcissable et produits réticulés
US6011123A (en) * 1996-11-20 2000-01-04 Jsr Corporation Curable resin composition and cured products
EP0921561A3 (fr) * 1997-12-02 2004-11-24 JSR Corporation Composition de revêtement pour la fabrication des couches
EP0932083A3 (fr) * 1998-01-20 2000-10-04 Shin-Etsu Chemical Co., Ltd. Composition de revêtement pour éléments d'électrisation et agent de véhiculation
US6100332A (en) * 1998-01-20 2000-08-08 Shin-Etsu Chemical Co., Ltd. Coating composition for electrifying members and electrophotographic carrier
EP1054047A3 (fr) * 1999-05-21 2001-10-10 JSR Corporation Composition de revêtement et films et verre revêtus par cette composition
EP1162247A3 (fr) * 2000-06-08 2002-04-17 Shin-Etsu Chemical Co., Ltd. Composition de revêtement, méthode pour revêtement et article revêtu
US6676740B2 (en) 2000-06-08 2004-01-13 Shin-Etsu Chemical Co., Ltd. Coating composition, coating method, and coated article
EP1726629A4 (fr) * 2004-03-15 2009-01-14 Tokuyama Corp Composition de revetement
WO2007137971A2 (fr) 2006-05-26 2007-12-06 Cht R. Beitlich Gmbh Concentrés diluables dans l'eau pour l'application de revêtements sur différents substrats
WO2007137971A3 (fr) * 2006-05-26 2008-04-17 Cht R Beitlich Gmbh Concentrés diluables dans l'eau pour l'application de revêtements sur différents substrats

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US5306759A (en) 1994-04-26
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DE69310402T2 (de) 1997-08-28

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